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dc.contributor.authorGuo, Hui-
dc.contributor.authorMann, Jennifer-
dc.contributor.authorGoh, Nicole S L-
dc.contributor.authorSmallwood, Natasha-
dc.identifier.citationInternal Medicine Journal 2020; 50(6): 748-752-
dc.description.abstractFibrotic interstitial lung disease (f-ILD) has a guarded prognosis, and the goal of therapy in advanced-stage disease should be symptom-based. Despite this, patients may still undergo burdensome investigation at the end of life. A retrospective audit was performed on 67 patients who died from f-ILD at the Royal Melbourne and Austin Hospitals between 2012 and 2016. Increased investigation burden was associated with lack of outpatient palliative care referral and documented advance care plan, and admission to a high-dependency unit. Eighteen per cent of patients underwent ongoing investigations after the institution of comfort care. These findings highlight the unmet end-of-life care needs of people with f-ILD.-
dc.subjectend-of-life care-
dc.subjectinterstitial lung disease-
dc.subjectpalliative care-
dc.subjectpulmonary fibrosis-
dc.titleInvestigation burden for patients with fibrotic interstitial lung disease at the end of life.-
dc.typeJournal Article-
dc.identifier.journaltitleInternal Medicine Journal-
dc.identifier.affiliationDepartment of Medicine (Royal Melbourne Hospital), University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, The Royal Melbourne Hospital, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Respiratory and Sleep Medicine, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationInstitute for Breathing and Sleep, Austin Health, Heidelberg, Victoria, Australiaen
Appears in Collections:Journal articles

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